Search
for
Sort by
Research 811–840 of 1000+
- Risk factors for prostate cancer: a case-control study investigating selected key exposures and their interactions with predisposition genes
- Modelling androgen synthesis and action during human sexual differentiation
- The childbearing years: hair diseases
- Book Reviews
- ANNOUNCEMENTS
- Quantitation of Hepatitis C Virus RNA
- Diagnosing Vascular Causes of Renal Failure
- Liver Cirrhosis and Circadian Rhythm
- Dermatological drugs, topical agents, and cosmetics
- PHILADELPHIA DERMATOLOGICAL SOCIETY
- Gene detection in a family with monilethrix and treatment with 5% topical minoxidil
- Aging‐associated perifollicular changes and calcium deposition in poodles
- Predominance of CD27-PD-1- Effector Memory T Cells Re-Expressing CD45RA Characterizes Treatment-Resistant Severe Alopecia Areata
- 236 Wnt/planar cell polarity impairment and the genetics of yellow nail syndrome
- DICENTRIC CHROMOSOME 14;18 PLUS TWO ADDITIONAL CNVs IN A GIRL WITH MICROFORM HOLOPROSENCEPHALY AND TURNER STIGMATA
- Two Different Mutations in the Same Codon of a Type II Hair Keratin (hHb6) in Patients with Monilethrix
- Circulating testosterone and feather-gene expression of receptors and metabolic enzymes in relation to melanin-based colouration in the barn owl
- The ATP sensitive potassium channel (KATP) is a novel target for migraine drug development
- Transcriptome analysis reveals the genetic basis underlying the formation and seasonal changes of nuptial pads in Rana chensinensis
- 1393 Lower proximal cup cells but not bulge stem cells regenerate hair follicles after chemotherapy injury
- Dermoscopic Assessment of Pityriasis Versicolor: A Cross-Sectional Observational Study
- An early diagnosis of trichorhinophalangeal syndrome type 1: a case report and a review of literature
- Complex X chromosome rearrangement associated with multiorgan autoimmunity
- De novo variation in ARID1B gene causes Coffin-Siris syndrome 1 in a Chinese family with excessive early-onset high myopia
- Endocrine abnormalities in ring chromosome 11: a case report and review of the literature
- Novel Compound Heterozygous Variants in the CDC6 Gene in a Russian Patient with Meier-Gorlin Syndrome
- Pregnancy and neonatal outcome with maternal exposure to finasteride: Case series
- Role of <i>foxn1</i> in <i>Xenopus laevis</i> thymopoiesis.
- Virilisation in a young woman: A case demonstrating the importance of co-located mental and primary healthcare
- Diagnosis and management of tinea infections.